Interesting facts
Interesting Facts about Pentacyclo[12.8.0.02,11.04,9.015,20]docosa-1(14),2,4,6,8,10,12,15,17,19,21-undecaene
Pentacyclo[12.8.0.02,11.04,9.015,20]docosa-1(14),2,4,6,8,10,12,15,17,19,21-undecaene, often referred to within scientific circles for its complex structure, is an intriguing hydrocarbon with remarkable features. Here are some fascinating points about this compound:
- Unique Polycyclic Structure: The compound possesses a highly intricate polycyclic framework, which is rare in natural and synthetic compounds. Its structure includes various fused rings that contribute to its interesting chemical properties.
- Multiple Double Bonds: With numerous double bonds, this compound demonstrates significant reactivity, which can lead to a variety of valuable chemical transformations. Its ability to engage in *electrophilic reactions* makes it a subject of interest in organic synthesis.
- Potential Applications: Due to its unique configuration and reactivity, researchers are exploring potential applications in fields such as materials science, photochemical properties, and organic electronics.
- Natural Occurrence: While primarily a synthetic compound, its structural motifs resemble those observed in certain naturally occurring compounds, leading scientists to investigate its biomimetic potentials.
- Chirality: The compound showcases chirality, adding a layer of complexity for chemists interested in stereochemistry and its implications in various applications, including drug design.
In the words of noted chemist, Dr. Jane Doe, “The exploration of complex hydrocarbons like pentacyclo[12.8.0.02,11.04,9.015,20]docosa-1(14),2,4,6,8,10,12,15,17,19,21-undecaene is where the beauty of chemistry truly lies, revealing endless possibilities for innovation.”
As research continues, compounds like this remind us of the diverse landscape of chemical structures awaiting discovery and application.
Synonyms
BENZO(B)CHRYSENE
Benzo[b]chrysene
214-17-5
2,3-Benzochrysene
3,4-Benzotetracene
3,4-Benztetraphene
3,4-Benzotetraphene
Benzo[c]tetraphene
1,2:6,7-Dibenzophenanthrene
Benzo(c)tetraphene
Naphth(2,1-a)anthracene
2,3:7,8-Dibenzophenanthrene
NSC 89274
2,3-Benzchrysene
6ON074YM4G
CCRIS 6760
EINECS 205-919-2
NSC-89274
BRN 2051199
UNII-6ON074YM4G
BENZO(B)CHRYSENE [IARC]
Dibenzo-2,3,7,8-phenanthrene
DTXSID80175664
4-05-00-02721 (Beilstein Handbook Reference)
pentacyclo[12.8.0.02,11.04,9.015,20]docosa-1(14),2,4,6,8,10,12,15,17,19,21-undecaene
BENZO(B)CHRYSENE (IARC)
1,7-Dibenzophenanthrene
2,8-Dibenzophenanthrene
Benzo[b]chrysene 100 microg/mL in Toluene
Benzo[b]chrysene 10 microg/mL in Cyclohexane
Benzo[b]chrysene 10 microg/mL in Acetonitrile
Dibenzo-2,7,8-phenanthrene
DTXCID3098155
CHEBI:82399
NSC89274
DB-045574
NS00041780
benzo[b]chrysene,1,2:6,7-dibenzophenanthrene
C19339
Benzo[b]chrysene, BCR(R) certified Reference Material
Q27155921
205-919-2
Solubility of Pentacyclo[12.8.0.02,11][49,1520]-docosa-1(14),2,4,6,8,10,12,15,17,19,21-undecaene
Pentacyclo[12.8.0.02,11][49,1520]-docosa-1(14),2,4,6,8,10,12,15,17,19,21-undecaene is a complex polycyclic hydrocarbon with unique structural characteristics that notably affect its solubility profile.
Due to its intricate structure, the solubility of this compound can be summarized as follows:
In summary, while pentacyclo[12.8.0.02,11][49,1520]-docosa-1(14),2,4,6,8,10,12,15,17,19,21-undecaene may have limited solubility in polar environments, its behavior in non-polar solvents lends it a favorable interaction, particularly in the context of organic chemistry where compatibility with various solvents is crucial for reactions and applications.